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匈牙利人群中缺血性卒中患者雌激素受体α(ESR1)PvuII和XbaI基因多态性

Estrogen receptor alpha (ESR1) PvuII and XbaI gene polymorphisms in ischemic stroke in a Hungarian population.

作者信息

Molvarec Attila, Széplaki Gábor, Kovács Margit, Széplaki Zoltán, Fazakas Adám, Prohászka Zoltán, Füst George, Karádi István

机构信息

Department of Obstetrics and Gynecology, Kútvölgyi Clinical Center, Semmelweis University, Budapest, Hungary.

出版信息

Clin Chim Acta. 2007 Jul;382(1-2):100-5. doi: 10.1016/j.cca.2007.04.003. Epub 2007 Apr 13.

Abstract

BACKGROUND

Ischemic stroke is a multifactorial disorder with genetic and environmental components. The aim of our study was to investigate whether two polymorphisms of the estrogen receptor alpha (ESR1) gene (ESR1 c.454-397T>C and c.454-351A>G) are associated with ischemic stroke in a Caucasian population from Hungary.

METHODS

One hundred and ninety-eight patients with ischemic stroke and 180 control subjects were enrolled in this case-control study. Ischemic stroke subtypes were categorized according to the Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification as large-artery atherosclerosis, small-artery occlusion, cardioembolism or stroke of other determined etiology. The ESR1 PvuII and XbaI genotypes were determined using the PCR-RFLP method.

RESULTS

There were no significant differences in the genotype, allele and haplotype frequencies of PvuII and XbaI polymorphisms between the group of patients with ischemic stroke and the control group. Furthermore, ESR1 PvuII and XbaI genotypes, alleles and haplotypes were not associated with any subtype of ischemic stroke.

CONCLUSIONS

We did not observe an association between ESR1 PvuII and XbaI gene polymorphisms and ischemic stroke or any subtype of ischemic stroke. However, further studies are needed to explore the complex interaction between environmental factors and ESR1 gene polymorphisms in the risk of ischemic stroke, particularly in ethnically different populations.

摘要

背景

缺血性中风是一种具有遗传和环境因素的多因素疾病。我们研究的目的是调查雌激素受体α(ESR1)基因的两种多态性(ESR1 c.454 - 397T>C和c.454 - 351A>G)是否与匈牙利白种人群中的缺血性中风相关。

方法

198例缺血性中风患者和180例对照受试者纳入了这项病例对照研究。缺血性中风亚型根据急性中风治疗中Org 10172试验(TOAST)分类为大动脉粥样硬化、小动脉闭塞、心源性栓塞或其他确定病因的中风。使用PCR - RFLP方法确定ESR1 PvuII和XbaI基因型。

结果

缺血性中风患者组和对照组之间PvuII和XbaI多态性的基因型、等位基因和单倍型频率没有显著差异。此外,ESR1 PvuII和XbaI基因型、等位基因和单倍型与缺血性中风的任何亚型均无关联。

结论

我们未观察到ESR1 PvuII和XbaI基因多态性与缺血性中风或缺血性中风的任何亚型之间存在关联。然而,需要进一步研究以探索环境因素与ESR1基因多态性在缺血性中风风险中的复杂相互作用,特别是在不同种族人群中。

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